Quality Manager

• Ability to work effectively in a cross-functional, matrixed environment, managing multiple tasks and priorities simultaneously.
• Bachelor’s degree in engineering, life sciences, or related field required; advanced degree or PMP certification preferred.
• Minimum 6 years of experience in biopharmaceutical or medical device industry, with at least 3 years in project management.
• Strong organizational skills, ability to thrive in a fast-paced environment, and comfortable managing high-visibility projects.
• Proficiency in Microsoft suite (Project, PowerPoint, SharePoint, Word, Excel, Outlook, Teams, OneNote, Visio, PowerBI) required.
• Previous experience in Quality/Manufacturing/Product Development or EU Medical Device Regulation (MDR) or CE Marking preferred.
• Experience interacting with Senior Management and connecting enterprise strategy to project objectives.
• Expertise in developing complex project timelines and defining project scope.
• Capability to convey project timelines visually using tools like Gantt Charts.
• Strong written and verbal communication skills, with a sense of urgency and accountability.

Job Type: Contract

Salary: Up to $75.00 per hour

Expected hours: 40 per week

Schedule:

• 8 hour shift

Work Location: In person